A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884860



Internal ID22659844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48758001..48766177hg38UCSC Ensembl
chrX:48616404..48624582hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg388177
hg198179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450526
Samples
Known GenesGLOD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884860
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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